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- W2086737101 abstract "We report here a premature female infant with agnathia, low-set but normally formed ears, a downward eye slant, choanal atresia and a cleft palate. She had severe respiratory distress and died despite maximum intervention at 5 days of age. Autopsy revealed situs inversus totalis; crossed fused renal ectopia; agnathia; normal thyroid, larynx, trachea, and bronchi; incomplete lobation of the lungs; immature pulmonary development with early hyaline membranes; and a normal central nervous system. This lack of significant central nervous system abnormalities distinguishes this infant from the majority of previously reported infants with agnathia and situs inversus." @default.
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- W2086737101 date "1992-09-01" @default.
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- W2086737101 title "A case of agnathia, situs inversus, and a normal central nervous system" @default.
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- W2086737101 doi "https://doi.org/10.1002/tera.1420460304" @default.
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